TABLE, PROAXIS 6988

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-20 for TABLE, PROAXIS 6988 manufactured by Mizuho Orthopedic Systems, Inc..

Event Text Entries

[183884824] It was reported the table was not flexed nor extended during the case. After the case there was redness that resulted in a pressure ulcer on the patient's chest.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2921578-2020-00005
MDR Report Key9606683
Report SourceUSER FACILITY
Date Received2020-01-20
Date of Report2020-01-20
Date of Event2020-01-10
Date Mfgr Received2020-01-10
Device Manufacturer Date2015-03-05
Date Added to Maude2020-01-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactANNE LEBLANC
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY CA 945871234
Manufacturer CountryUS
Manufacturer Postal945871234
Manufacturer Phone5104291500
Manufacturer G1MIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Street30031 AHERN AVENUE
Manufacturer CityUNION CITY CA 945871234
Manufacturer CountryUS
Manufacturer Postal Code945871234
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTABLE, PROAXIS
Generic NameSURGICAL OPERATING TABLE
Product CodeJEA
Date Received2020-01-20
Model Number6988
Catalog Number6988
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMIZUHO ORTHOPEDIC SYSTEMS, INC.
Manufacturer Address30031 AHERN AVENUE UNION CITY CA 945871234 US 945871234


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-20

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